Skip to main content
Journal cover image

Cytogenetic and molecular analysis of an unusual case of acute promyelocytic leukemia with a t(15;17;17)(q22;q23;q21).

Publication ,  Journal Article
Tirado, CA; Golembiewski-Ruiz, V; Horvatinovich, J; Moore, JO; Buckley, PJ; Stenzel, TT; Goodman, BK
Published in: Cancer Genet Cytogenet
August 2003

We present a 52-year-old female with a clinical history of acute myelocytic leukemia, probable acute promyelocytic leukemia (APL). Flow cytometry results were somewhat unusual. Specifically, the promyelocytic population showed partial positivity for antigens not usually expressed in APL (HLA-DR and CD117). The interpretation of these results was that the abnormal population contained a proportion of very early promyeolocytes that had not completely lost all their "precursor" antigens. Cytogenetic analysis of a bone marrow aspirate showed a t(15:17;17)(q22;q23;q21) in all cells analyzed. Fluorescence in situ hybridization (FISH) analysis using the PML-RARA DNA probe showed a positive signal pattern (fusion) in 100% of 200 total interphase and metaphase cells examined, confirming the presence of the PML-RARA rearrangement. Multicolor FISH, which produces 24 colors to differentiate all chromosomes in a single hybridization, was applied. This study confirmed the cytogenetic interpretation of the rearrangement. No material from any other chromosome was detected on the second smaller derivative chromosome 17. Additional studies using the RARA(17q21) break-apart DNA FISH probe showed that 17q21 (RARA) was not rearranged on the derivative chromosome 17 that received the q22-->qter segment from chromosome 15. The RARA locus on the smaller derivative 17 was the allele involved in the fusion in this three-way rearrangement. The signal pattern was consistent in 100% of interphase and metaphase cells scored. This unusual t(15;17;17) prompted us to investigate further using reverse-transcription polymerase chain reaction with primers from the 3' and 5' regions of both the RARA and PML loci. These studies showed that the PML-RARA fusion was present, but the complementary fusion RARA-PML, which is usually detectable, was absent. The patient is responding well to standard treatment protocols.

Duke Scholars

Published In

Cancer Genet Cytogenet

DOI

ISSN

0165-4608

Publication Date

August 2003

Volume

145

Issue

1

Start / End Page

31 / 37

Location

United States

Related Subject Headings

  • Translocation, Genetic
  • Oncology & Carcinogenesis
  • Middle Aged
  • Leukemia, Promyelocytic, Acute
  • Karyotyping
  • In Situ Hybridization, Fluorescence
  • Humans
  • Flow Cytometry
  • Female
  • Chromosomes, Human, Pair 17
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Tirado, C. A., Golembiewski-Ruiz, V., Horvatinovich, J., Moore, J. O., Buckley, P. J., Stenzel, T. T., & Goodman, B. K. (2003). Cytogenetic and molecular analysis of an unusual case of acute promyelocytic leukemia with a t(15;17;17)(q22;q23;q21). Cancer Genet Cytogenet, 145(1), 31–37. https://doi.org/10.1016/s0165-4608(03)00027-x
Tirado, C. A., V. Golembiewski-Ruiz, J. Horvatinovich, J. O. Moore, P. J. Buckley, T. T. Stenzel, and B. K. Goodman. “Cytogenetic and molecular analysis of an unusual case of acute promyelocytic leukemia with a t(15;17;17)(q22;q23;q21).Cancer Genet Cytogenet 145, no. 1 (August 2003): 31–37. https://doi.org/10.1016/s0165-4608(03)00027-x.
Tirado CA, Golembiewski-Ruiz V, Horvatinovich J, Moore JO, Buckley PJ, Stenzel TT, et al. Cytogenetic and molecular analysis of an unusual case of acute promyelocytic leukemia with a t(15;17;17)(q22;q23;q21). Cancer Genet Cytogenet. 2003 Aug;145(1):31–7.
Tirado, C. A., et al. “Cytogenetic and molecular analysis of an unusual case of acute promyelocytic leukemia with a t(15;17;17)(q22;q23;q21).Cancer Genet Cytogenet, vol. 145, no. 1, Aug. 2003, pp. 31–37. Pubmed, doi:10.1016/s0165-4608(03)00027-x.
Tirado CA, Golembiewski-Ruiz V, Horvatinovich J, Moore JO, Buckley PJ, Stenzel TT, Goodman BK. Cytogenetic and molecular analysis of an unusual case of acute promyelocytic leukemia with a t(15;17;17)(q22;q23;q21). Cancer Genet Cytogenet. 2003 Aug;145(1):31–37.
Journal cover image

Published In

Cancer Genet Cytogenet

DOI

ISSN

0165-4608

Publication Date

August 2003

Volume

145

Issue

1

Start / End Page

31 / 37

Location

United States

Related Subject Headings

  • Translocation, Genetic
  • Oncology & Carcinogenesis
  • Middle Aged
  • Leukemia, Promyelocytic, Acute
  • Karyotyping
  • In Situ Hybridization, Fluorescence
  • Humans
  • Flow Cytometry
  • Female
  • Chromosomes, Human, Pair 17